| HNF1beta bookmarking involves Topoisomerase 1 activation and DNA topology relaxation in mitotic chromatin. | HNF1β bookmarking involves Topoisomerase 1 activation and DNA topology relaxation in mitotic chromatin.
Bagattin A, Tammaccaro SL, Chiral M, Makinistoglu MP, Zimmermann N, Lerner J, Garbay S, Kuperwasser N, Pontoglio M. | 11/1/2024 |
| HNF1B Transcription Factor: Key Regulator in Renal Physiology and Pathogenesis. | HNF1B Transcription Factor: Key Regulator in Renal Physiology and Pathogenesis.
Sánchez-Cazorla E, Carrera N, García-González MÁ., Free PMC Article | 10/25/2024 |
| A Korean Family Presenting with Renal Cysts and Maturity-Onset Diabetes of the Young Caused by a Novel In-Frame Deletion of HNF1B. | A Korean Family Presenting with Renal Cysts and Maturity-Onset Diabetes of the Young Caused by a Novel In-Frame Deletion of HNF1B.
Han JY, Gwack J, Kim TY, Park J., Free PMC Article | 10/8/2024 |
| Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations. | Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations.
Bantounas I, Rooney KM, Lopes FM, Tengku F, Woods S, Zeef LAH, Lin IH, Kuba SY, Bates N, Hummelgaard S, Hillman KA, Cereghini S, Woolf AS, Kimber SJ., Free PMC Article | 06/25/2024 |
| Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions. | Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.
Verscaj CP, Velez-Bartolomei F, Bodle E, Chan K, Lyons MJ, Thorson W, Tan WH, Rodig N, Graham JM Jr, Peron A, Quintero-Rivera F, Zackai EH, Thomas MA, Stevens CA, Adam MP, Bird LM, Jones MC, Matalon DR. | 02/20/2024 |
| Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion. | Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion.
Chen CP, Wu FT, Pan YT, Wu PS, Wang W. | 01/27/2024 |
| Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia. | Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia.
Wang Y, Xiao X, Lin Q, Song R, Wang X, Liang Y, Chen J, Luan X, Zhou Z, Xiao Y, Xue Y, Hu J., Free PMC Article | 01/8/2024 |
| Dysregulation of HNF1B/Clusterin axis enhances disease progression in a highly aggressive subset of pancreatic cancer patients. | Dysregulation of HNF1B/Clusterin axis enhances disease progression in a highly aggressive subset of pancreatic cancer patients.
Yang S, Tang W, Azizian A, Gaedcke J, Ströbel P, Wang L, Cawley H, Ohara Y, Valenzuela P, Zhang L, Lal T, Sinha S, Rupin E, Hanna N, Ghadimi BM, Hussain SP., Free PMC Article | 04/26/2023 |
| HNF1B-driven three-dimensional chromatin structure for molecular classification in pancreatic cancers. | HNF1B-driven three-dimensional chromatin structure for molecular classification in pancreatic cancers.
Kato H, Tateishi K, Iwadate D, Yamamoto K, Fujiwara H, Nakatsuka T, Kudo Y, Hayakawa Y, Ijichi H, Otsuka M, Kishikawa T, Takahashi R, Miyabayashi K, Nakai Y, Hirata Y, Toyoda A, Morishita S, Fujishiro M., Free PMC Article | 04/5/2023 |
| Functional genomics analysis identifies loss of HNF1B function as a cause of Mayer-Rokitansky-Kuster-Hauser syndrome. | Functional genomics analysis identifies loss of HNF1B function as a cause of Mayer-Rokitansky-Küster-Hauser syndrome.
Thomson E, Tran M, Robevska G, Ayers K, van der Bergen J, Gopalakrishnan Bhaskaran P, Haan E, Cereghini S, Vash-Margita A, Margetts M, Hensley A, Nguyen Q, Sinclair A, Koopman P, Pelosi E., Free PMC Article | 03/11/2023 |
| HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes. | HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes.
Grand K, Stoltz M, Rizzo L, Röck R, Kaminski MM, Salinas G, Getwan M, Naert T, Pichler R, Lienkamp SS., Free PMC Article | 03/7/2023 |
| The Landscape of HNF1B Deficiency: A Syndrome Not Yet Fully Explored. | The Landscape of HNF1B Deficiency: A Syndrome Not Yet Fully Explored.
Gambella A, Kalantari S, Cadamuro M, Quaglia M, Delvecchio M, Fabris L, Pinon M., Free PMC Article | 02/11/2023 |
| Two cases of fetal hyperechogenic kidneys who had HNF1-beta gene variation. | Two cases of fetal hyperechogenic kidneys who had HNF1-β gene variation.
Li H, Chen C, Tu J, Geng H, Lin T. | 01/28/2023 |
| HNF1beta-associated cyst development and electrolyte disturbances are not explained by BAIAP2L2 expression. | HNF1β-associated cyst development and electrolyte disturbances are not explained by BAIAP2L2 expression.
Tholen LE, Schigt H, Kleuskens SGE, Bos C, Spruijt CG, Willemsen B, Vermeulen M, Hoenderop JGJ, de Baaij JHF. | 12/31/2022 |
| P504S/alpha-methylacyl-CoA racemase, HNF1beta and napsin A in morular metaplasia and clear cell carcinoma of the endometrium: An immunohistochemical analysis. | P504S/alpha-methylacyl-CoA racemase, HNF1β and napsin A in morular metaplasia and clear cell carcinoma of the endometrium: An immunohistochemical analysis.
Arciuolo D, Travaglino A, Raffone A, Santoro A, Inzani F, Piermattei A, Bui L, Scaglione G, D'Alessandris N, Valente M, Fulgione C, Guida M, Mollo A, Insabato L, Zannoni GF. | 08/13/2022 |
| MNX1-HNF1B Axis Is Indispensable for Intraductal Papillary Mucinous Neoplasm Lineages. | MNX1-HNF1B Axis Is Indispensable for Intraductal Papillary Mucinous Neoplasm Lineages.
Kato H, Tateishi K, Fujiwara H, Nakatsuka T, Yamamoto K, Kudo Y, Hayakawa Y, Nakagawa H, Tanaka Y, Ijichi H, Otsuka M, Iwadate D, Oyama H, Kanai S, Noguchi K, Suzuki T, Sato T, Hakuta R, Ishigaki K, Saito K, Saito T, Takahara N, Kishikawa T, Hamada T, Takahashi R, Miyabayashi K, Mizuno S, Kogure H, Nakai Y, Hirata Y, Toyoda A, Ichikawa K, Qu W, Morishita S, Arita J, Tanaka M, Ushiku T, Hasegawa K, Fujishiro M, Koike K. | 05/14/2022 |
| Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study. | Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study.
Małachowska B, Janikiewicz J, Pietrowska K, Wyka K, Madzio J, Wypyszczak K, Tkaczyk M, Chrul S, Zwiech R, Hogendorf A, Małecki MT, Borowiec M, Krętowski A, Młynarski W, Dobrzyń A, Ciborowski M, Fendler W., Free PMC Article | 04/2/2022 |
| Modeling HNF1B-associated monogenic diabetes using human iPSCs reveals an early stage impairment of the pancreatic developmental program. | Modeling HNF1B-associated monogenic diabetes using human iPSCs reveals an early stage impairment of the pancreatic developmental program.
El-Khairi R, Olszanowski E, Muraro D, Madrigal P, Tilgner K, Chhatriwala M, Vyas S, Chia CY, Vallier L, Rodríguez-Seguí SA., Free PMC Article | 03/12/2022 |
| Comprehensive quantitative analysis of alternative splicing variants reveals the HNF1B mRNA splicing pattern in various tumour and non-tumour tissues. | Comprehensive quantitative analysis of alternative splicing variants reveals the HNF1B mRNA splicing pattern in various tumour and non-tumour tissues.
Hojny J, Michalkova R, Krkavcova E, Bui QH, Bartu M, Nemejcova K, Kalousova M, Kleiblova P, Dundr P, Struzinska I., Free PMC Article | 02/26/2022 |
| A Review of Functional Characterization of Single Amino Acid Change Mutations in HNF Transcription Factors in MODY Pathogenesis. | A Review of Functional Characterization of Single Amino Acid Change Mutations in HNF Transcription Factors in MODY Pathogenesis.
Çubuk H, Yalçın Çapan Ö. | 12/25/2021 |
| Hepatocyte nuclear factor-1beta shapes the energetic homeostasis of kidney tubule cells. | Hepatocyte nuclear factor-1β shapes the energetic homeostasis of kidney tubule cells.
Piedrafita A, Balayssac S, Casemayou A, Saulnier-Blache JS, Lucas A, Iacovoni JS, Breuil B, Chauveau D, Decramer S, Malet-Martino M, Schanstra JP, Faguer S. | 11/13/2021 |
| Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the Young. | Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the Young.
Berberich AJ, Wang J, Cao H, McIntyre AD, Spaic T, Miller DB, Stock S, Huot C, Stein R, Knoll J, Yang P, Robinson JF, Hegele RA. | 10/16/2021 |
| Chromatin accessibility of kidney tubular cells under stress reveals key transcription factor mediating acute and chronic kidney disease. | Chromatin accessibility of kidney tubular cells under stress reveals key transcription factor mediating acute and chronic kidney disease.
Xing Y, Wang Q, Zhang J, Li W, Duan A, Yang J, Liu Z. | 10/2/2021 |
| HNF1beta is a sensitive and specific novel marker for yolk sac tumor: a tissue microarray analysis of 601 testicular germ cell tumors. | HNF1β is a sensitive and specific novel marker for yolk sac tumor: a tissue microarray analysis of 601 testicular germ cell tumors.
Gallo A, Fankhauser C, Hermanns T, Beyer J, Christiansen A, Moch H, Bode PK. | 08/28/2021 |
| Napsin-A and AMACR are Superior to HNF-1beta in Distinguishing Between Mesonephric Carcinomas and Clear Cell Carcinomas of the Gynecologic Tract. | Napsin-A and AMACR are Superior to HNF-1β in Distinguishing Between Mesonephric Carcinomas and Clear Cell Carcinomas of the Gynecologic Tract.
Pors J, Segura S, Cheng A, Ji JX, Tessier-Cloutier B, Cochrane D, Fix DJ, Park K, Gilks B, Hoang L., Free PMC Article | 08/7/2021 |